JP2005533034A5 - - Google Patents
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- Publication number
- JP2005533034A5 JP2005533034A5 JP2004508808A JP2004508808A JP2005533034A5 JP 2005533034 A5 JP2005533034 A5 JP 2005533034A5 JP 2004508808 A JP2004508808 A JP 2004508808A JP 2004508808 A JP2004508808 A JP 2004508808A JP 2005533034 A5 JP2005533034 A5 JP 2005533034A5
- Authority
- JP
- Japan
- Prior art keywords
- guanidine
- oxo
- dihydro
- isoindol
- acetyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims description 23
- -1 CO 2 H Chemical group 0.000 claims description 6
- 125000004432 carbon atoms Chemical group C* 0.000 claims 46
- 150000001875 compounds Chemical class 0.000 claims 24
- 150000003839 salts Chemical class 0.000 claims 18
- 239000011780 sodium chloride Substances 0.000 claims 18
- 230000002265 prevention Effects 0.000 claims 17
- 125000000217 alkyl group Chemical group 0.000 claims 16
- 201000010099 disease Diseases 0.000 claims 13
- 229910052739 hydrogen Inorganic materials 0.000 claims 13
- 239000001257 hydrogen Substances 0.000 claims 13
- 239000003814 drug Substances 0.000 claims 11
- 210000000056 organs Anatomy 0.000 claims 11
- 206010016654 Fibrosis Diseases 0.000 claims 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims 9
- 230000004761 fibrosis Effects 0.000 claims 9
- 239000008194 pharmaceutical composition Substances 0.000 claims 9
- 239000004480 active ingredient Substances 0.000 claims 8
- 230000035939 shock Effects 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 7
- 210000001519 tissues Anatomy 0.000 claims 7
- 210000003169 Central Nervous System Anatomy 0.000 claims 6
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 6
- 230000001154 acute Effects 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 230000001684 chronic Effects 0.000 claims 5
- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- GTIIVHODSNYECK-UHFFFAOYSA-N 1,1,1-trifluoropropane Chemical group [CH2]CC(F)(F)F GTIIVHODSNYECK-UHFFFAOYSA-N 0.000 claims 4
- PJJJBBJSCAKJQF-UHFFFAOYSA-N Guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 claims 4
- 206010061255 Ischaemia Diseases 0.000 claims 4
- 208000001072 Type 2 Diabetes Mellitus Diseases 0.000 claims 4
- 230000001451 cardiotoxic Effects 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 238000001356 surgical procedure Methods 0.000 claims 4
- 206010027476 Metastasis Diseases 0.000 claims 3
- 208000003663 Ventricular Fibrillation Diseases 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 125000003282 alkyl amino group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 201000006233 congestive heart failure Diseases 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- 230000000302 ischemic Effects 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 206010002199 Anaphylactic shock Diseases 0.000 claims 2
- 206010002383 Angina pectoris Diseases 0.000 claims 2
- 206010002855 Anxiety Diseases 0.000 claims 2
- 206010057666 Anxiety disease Diseases 0.000 claims 2
- 206010003119 Arrhythmia Diseases 0.000 claims 2
- 206010003210 Arteriosclerosis Diseases 0.000 claims 2
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims 2
- 230000037227 Blood Loss Effects 0.000 claims 2
- 206010007521 Cardiac arrhythmias Diseases 0.000 claims 2
- 208000003495 Coccidiosis Diseases 0.000 claims 2
- 206010010904 Convulsion Diseases 0.000 claims 2
- 206010012601 Diabetes mellitus Diseases 0.000 claims 2
- 206010048554 Endothelial dysfunction Diseases 0.000 claims 2
- 208000007530 Essential Hypertension Diseases 0.000 claims 2
- 206010020718 Hyperplasia Diseases 0.000 claims 2
- 206010020772 Hypertension Diseases 0.000 claims 2
- 206010022114 Injury Diseases 0.000 claims 2
- 206010022562 Intermittent claudication Diseases 0.000 claims 2
- 206010023076 Isosporiasis Diseases 0.000 claims 2
- 206010023421 Kidney fibrosis Diseases 0.000 claims 2
- ZCSHNCUQKCANBX-UHFFFAOYSA-N Lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 claims 2
- 210000004185 Liver Anatomy 0.000 claims 2
- 108009000252 Lung fibrosis Proteins 0.000 claims 2
- 208000010125 Myocardial Infarction Diseases 0.000 claims 2
- 208000003067 Myocardial Ischemia Diseases 0.000 claims 2
- 229910003827 NRaRb Inorganic materials 0.000 claims 2
- 210000001428 Peripheral Nervous System Anatomy 0.000 claims 2
- 206010036790 Productive cough Diseases 0.000 claims 2
- 210000002307 Prostate Anatomy 0.000 claims 2
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims 2
- 206010061920 Psychotic disease Diseases 0.000 claims 2
- 208000005069 Pulmonary Fibrosis Diseases 0.000 claims 2
- 210000003802 Sputum Anatomy 0.000 claims 2
- 208000007536 Thrombosis Diseases 0.000 claims 2
- 210000001685 Thyroid Gland Anatomy 0.000 claims 2
- 230000032683 aging Effects 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 2
- 230000036506 anxiety Effects 0.000 claims 2
- 201000001320 atherosclerosis Diseases 0.000 claims 2
- 230000001580 bacterial Effects 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 230000004663 cell proliferation Effects 0.000 claims 2
- 230000036461 convulsion Effects 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- 201000010238 heart disease Diseases 0.000 claims 2
- 200000000018 inflammatory disease Diseases 0.000 claims 2
- 150000002632 lipids Chemical class 0.000 claims 2
- 244000144972 livestock Species 0.000 claims 2
- 201000004792 malaria Diseases 0.000 claims 2
- 230000002503 metabolic Effects 0.000 claims 2
- 125000004433 nitrogen atoms Chemical group N* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 230000002093 peripheral Effects 0.000 claims 2
- 230000000607 poisoning Effects 0.000 claims 2
- 231100000572 poisoning Toxicity 0.000 claims 2
- 244000144977 poultry Species 0.000 claims 2
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 230000001568 sexual Effects 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 238000002054 transplantation Methods 0.000 claims 2
- 230000002792 vascular Effects 0.000 claims 2
- KLNVEUWLOSAYAN-UHFFFAOYSA-N 1-[2-(diaminomethylideneamino)-2-oxoethyl]-2-(2-methylpropyl)-3-oxo-1H-isoindole-4-carboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 KLNVEUWLOSAYAN-UHFFFAOYSA-N 0.000 claims 1
- LJVDTBANFYSGBK-UHFFFAOYSA-N 1-[2-(diaminomethylideneamino)-2-oxoethyl]-2-(2-methylpropyl)-3-oxo-1H-isoindole-5-carboxylic acid Chemical compound C1=C(C(O)=O)C=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 LJVDTBANFYSGBK-UHFFFAOYSA-N 0.000 claims 1
- KWKPPZVLRABURT-UHFFFAOYSA-N 1-ethoxyethenoxy(trimethyl)silane Chemical group CCOC(=C)O[Si](C)(C)C KWKPPZVLRABURT-UHFFFAOYSA-N 0.000 claims 1
- QQAIWKHSYOXLLE-UHFFFAOYSA-N 2-(2-benzyl-3-oxo-1H-isoindol-1-yl)-N-(diaminomethylidene)acetamide Chemical compound O=C1C2=CC=CC=C2C(CC(=O)NC(=N)N)N1CC1=CC=CC=C1 QQAIWKHSYOXLLE-UHFFFAOYSA-N 0.000 claims 1
- STAMYLAXOLXWTN-UHFFFAOYSA-N 2-(2-butyl-3-oxo-1H-isoindol-1-yl)-N-(diaminomethylidene)propanamide Chemical compound C1=CC=C2C(=O)N(CCCC)C(C(C)C(=O)NC(N)=N)C2=C1 STAMYLAXOLXWTN-UHFFFAOYSA-N 0.000 claims 1
- NWQDLXHKESKFCQ-GFCCVEGCSA-N 2-[(1R)-2-(cyclopropylmethyl)-3-oxo-6-(trifluoromethyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound N1([C@@H](C2=CC(=CC=C2C1=O)C(F)(F)F)CC(=O)NC(=N)N)CC1CC1 NWQDLXHKESKFCQ-GFCCVEGCSA-N 0.000 claims 1
- QJELXFOTUYLTBZ-LLVKDONJSA-N 2-[(1R)-5-chloro-3-oxo-2-(4,4,4-trifluorobutyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound ClC1=CC=C2[C@@H](CC(=O)NC(=N)N)N(CCCC(F)(F)F)C(=O)C2=C1 QJELXFOTUYLTBZ-LLVKDONJSA-N 0.000 claims 1
- YWMDULJDQPDAIW-GFCCVEGCSA-N 2-[(1R)-6-chloro-2-(cyclopropylmethyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound N1([C@@H](C2=CC(Cl)=CC=C2C1=O)CC(=O)NC(=N)N)CC1CC1 YWMDULJDQPDAIW-GFCCVEGCSA-N 0.000 claims 1
- IHSHGVSESIJPKM-LLVKDONJSA-N 2-[(1R)-6-chloro-3-oxo-2-(4,4,4-trifluorobutyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(Cl)C=C2[C@@H](CC(=O)NC(=N)N)N(CCCC(F)(F)F)C(=O)C2=C1 IHSHGVSESIJPKM-LLVKDONJSA-N 0.000 claims 1
- NWQDLXHKESKFCQ-LBPRGKRZSA-N 2-[(1S)-2-(cyclopropylmethyl)-3-oxo-6-(trifluoromethyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound N1([C@H](C2=CC(=CC=C2C1=O)C(F)(F)F)CC(=O)NC(=N)N)CC1CC1 NWQDLXHKESKFCQ-LBPRGKRZSA-N 0.000 claims 1
- QJELXFOTUYLTBZ-NSHDSACASA-N 2-[(1S)-5-chloro-3-oxo-2-(4,4,4-trifluorobutyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound ClC1=CC=C2[C@H](CC(=O)NC(=N)N)N(CCCC(F)(F)F)C(=O)C2=C1 QJELXFOTUYLTBZ-NSHDSACASA-N 0.000 claims 1
- YWMDULJDQPDAIW-LBPRGKRZSA-N 2-[(1S)-6-chloro-2-(cyclopropylmethyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound N1([C@H](C2=CC(Cl)=CC=C2C1=O)CC(=O)NC(=N)N)CC1CC1 YWMDULJDQPDAIW-LBPRGKRZSA-N 0.000 claims 1
- IHSHGVSESIJPKM-NSHDSACASA-N 2-[(1S)-6-chloro-3-oxo-2-(4,4,4-trifluorobutyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(Cl)C=C2[C@H](CC(=O)NC(=N)N)N(CCCC(F)(F)F)C(=O)C2=C1 IHSHGVSESIJPKM-NSHDSACASA-N 0.000 claims 1
- PGXZQSDCCLHNCR-UHFFFAOYSA-N 2-[2-(cyclopropylmethyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)-2-methylpropanamide Chemical compound O=C1C2=CC=CC=C2C(C(C)(C)C(=O)NC(N)=N)N1CC1CC1 PGXZQSDCCLHNCR-UHFFFAOYSA-N 0.000 claims 1
- QRJBIYOIRJRIBT-UHFFFAOYSA-N 2-[2-(cyclopropylmethyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound O=C1C2=CC=CC=C2C(CC(=O)NC(=N)N)N1CC1CC1 QRJBIYOIRJRIBT-UHFFFAOYSA-N 0.000 claims 1
- LDYKBVRWVXLTAU-UHFFFAOYSA-N 2-[2-(cyclopropylmethyl)-3-oxo-5-(trifluoromethyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound O=C1C2=CC(C(F)(F)F)=CC=C2C(CC(=O)NC(=N)N)N1CC1CC1 LDYKBVRWVXLTAU-UHFFFAOYSA-N 0.000 claims 1
- NWQDLXHKESKFCQ-UHFFFAOYSA-N 2-[2-(cyclopropylmethyl)-3-oxo-6-(trifluoromethyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound O=C1C2=CC=C(C(F)(F)F)C=C2C(CC(=O)NC(=N)N)N1CC1CC1 NWQDLXHKESKFCQ-UHFFFAOYSA-N 0.000 claims 1
- QDMKCZZDBOKEBB-UHFFFAOYSA-N 2-[4-amino-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=CC(N)=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 QDMKCZZDBOKEBB-UHFFFAOYSA-N 0.000 claims 1
- CLPIMAABPKFTAW-UHFFFAOYSA-N 2-[5-amino-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(N)C=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 CLPIMAABPKFTAW-UHFFFAOYSA-N 0.000 claims 1
- SARVGKIWDAYOIE-UHFFFAOYSA-N 2-[5-bromo-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(Br)C=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 SARVGKIWDAYOIE-UHFFFAOYSA-N 0.000 claims 1
- OHKBUGGZURTKCN-UHFFFAOYSA-N 2-[5-chloro-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(Cl)C=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 OHKBUGGZURTKCN-UHFFFAOYSA-N 0.000 claims 1
- POKMRWNLJJKTRY-UHFFFAOYSA-N 2-[5-chloro-2-(cyclopropylmethyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound O=C1C2=CC(Cl)=CC=C2C(CC(=O)NC(=N)N)N1CC1CC1 POKMRWNLJJKTRY-UHFFFAOYSA-N 0.000 claims 1
- NLMUZTFCTZRORA-UHFFFAOYSA-N 2-[5-chloro-3-oxo-2-(2,2,2-trifluoroethyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound ClC1=CC=C2C(CC(=O)NC(=N)N)N(CC(F)(F)F)C(=O)C2=C1 NLMUZTFCTZRORA-UHFFFAOYSA-N 0.000 claims 1
- WKPMPKRRVOLACW-UHFFFAOYSA-N 2-[5-chloro-3-oxo-2-(3,3,3-trifluoropropyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound ClC1=CC=C2C(CC(=O)NC(=N)N)N(CCC(F)(F)F)C(=O)C2=C1 WKPMPKRRVOLACW-UHFFFAOYSA-N 0.000 claims 1
- QJELXFOTUYLTBZ-UHFFFAOYSA-N 2-[5-chloro-3-oxo-2-(4,4,4-trifluorobutyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound ClC1=CC=C2C(CC(=O)NC(=N)N)N(CCCC(F)(F)F)C(=O)C2=C1 QJELXFOTUYLTBZ-UHFFFAOYSA-N 0.000 claims 1
- HNSOCCBNBGMEKO-UHFFFAOYSA-N 2-[5-tert-butyl-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(C(C)(C)C)C=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 HNSOCCBNBGMEKO-UHFFFAOYSA-N 0.000 claims 1
- ITDJXMAXHZSIFF-UHFFFAOYSA-N 2-[6-amino-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound NC1=CC=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 ITDJXMAXHZSIFF-UHFFFAOYSA-N 0.000 claims 1
- SFSZEIMFRMGQTA-UHFFFAOYSA-N 2-[6-bromo-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound BrC1=CC=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 SFSZEIMFRMGQTA-UHFFFAOYSA-N 0.000 claims 1
- NASPYBSHSKLICW-UHFFFAOYSA-N 2-[6-chloro-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound ClC1=CC=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 NASPYBSHSKLICW-UHFFFAOYSA-N 0.000 claims 1
- YWMDULJDQPDAIW-UHFFFAOYSA-N 2-[6-chloro-2-(cyclopropylmethyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound O=C1C2=CC=C(Cl)C=C2C(CC(=O)NC(=N)N)N1CC1CC1 YWMDULJDQPDAIW-UHFFFAOYSA-N 0.000 claims 1
- NABZEVACEANYPP-UHFFFAOYSA-N 2-[6-chloro-3-oxo-2-(2,2,2-trifluoroethyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(Cl)C=C2C(CC(=O)NC(=N)N)N(CC(F)(F)F)C(=O)C2=C1 NABZEVACEANYPP-UHFFFAOYSA-N 0.000 claims 1
- ZCIHGBJPBCCQSS-UHFFFAOYSA-N 2-[6-chloro-3-oxo-2-(3,3,3-trifluoropropyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(Cl)C=C2C(CC(=O)NC(=N)N)N(CCC(F)(F)F)C(=O)C2=C1 ZCIHGBJPBCCQSS-UHFFFAOYSA-N 0.000 claims 1
- IHSHGVSESIJPKM-UHFFFAOYSA-N 2-[6-chloro-3-oxo-2-(4,4,4-trifluorobutyl)-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound C1=C(Cl)C=C2C(CC(=O)NC(=N)N)N(CCCC(F)(F)F)C(=O)C2=C1 IHSHGVSESIJPKM-UHFFFAOYSA-N 0.000 claims 1
- IXLFTXVHUXKCOF-UHFFFAOYSA-N 2-[6-tert-butyl-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound CC(C)(C)C1=CC=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 IXLFTXVHUXKCOF-UHFFFAOYSA-N 0.000 claims 1
- VNWITPYUVAYBCW-UHFFFAOYSA-N 2-[7-amino-2-(2-methylpropyl)-3-oxo-1H-isoindol-1-yl]-N-(diaminomethylidene)acetamide Chemical compound O=C1N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1C=CC=C2N VNWITPYUVAYBCW-UHFFFAOYSA-N 0.000 claims 1
- UJSLWLNGWTWSFN-UHFFFAOYSA-N 3-[2-(diaminomethylideneamino)-2-oxoethyl]-2-(2-methylpropyl)-1-oxo-3H-isoindole-4-carboxylic acid Chemical compound O=C1N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1C=CC=C2C(O)=O UJSLWLNGWTWSFN-UHFFFAOYSA-N 0.000 claims 1
- HJEYGVQONPNOIU-UHFFFAOYSA-N 3-[2-(diaminomethylideneamino)-2-oxoethyl]-2-(2-methylpropyl)-1-oxo-3H-isoindole-5-carboxylic acid Chemical compound OC(=O)C1=CC=C2C(=O)N(CC(C)C)C(CC(=O)NC(N)=N)C2=C1 HJEYGVQONPNOIU-UHFFFAOYSA-N 0.000 claims 1
- 206010007554 Cardiac failure Diseases 0.000 claims 1
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 1
- 229940039227 DIAGNOSTIC AGENTS Drugs 0.000 claims 1
- 206010019280 Heart failure Diseases 0.000 claims 1
- 239000002841 Lewis acid Substances 0.000 claims 1
- VRJWRXOULMHABM-UHFFFAOYSA-N N-(diaminomethylidene)-2-(2-ethyl-3-oxo-1H-isoindol-1-yl)acetamide Chemical compound C1=CC=C2C(=O)N(CC)C(CC(=O)NC(N)=N)C2=C1 VRJWRXOULMHABM-UHFFFAOYSA-N 0.000 claims 1
- XDOIXOUBPPKXCU-UHFFFAOYSA-N N-(diaminomethylidene)-2-(2-methyl-3-oxo-1H-isoindol-1-yl)acetamide Chemical compound C1=CC=C2C(=O)N(C)C(CC(=O)NC(N)=N)C2=C1 XDOIXOUBPPKXCU-UHFFFAOYSA-N 0.000 claims 1
- MGRUNSIBUNAFKA-UHFFFAOYSA-N N-(diaminomethylidene)-2-(3-oxo-1,2-dihydroisoindol-1-yl)acetamide Chemical compound C1=CC=C2C(CC(=O)NC(=N)N)NC(=O)C2=C1 MGRUNSIBUNAFKA-UHFFFAOYSA-N 0.000 claims 1
- FVUZKVAUHNNMGX-UHFFFAOYSA-N N-(diaminomethylidene)-2-(3-oxo-2-propan-2-yl-1H-isoindol-1-yl)acetamide Chemical compound C1=CC=C2C(=O)N(C(C)C)C(CC(=O)NC(N)=N)C2=C1 FVUZKVAUHNNMGX-UHFFFAOYSA-N 0.000 claims 1
- TXIRKRZTAUCXFR-UHFFFAOYSA-N N-(diaminomethylidene)-2-(3-oxo-2-propyl-1H-isoindol-1-yl)acetamide Chemical compound C1=CC=C2C(=O)N(CCC)C(CC(=O)NC(N)=N)C2=C1 TXIRKRZTAUCXFR-UHFFFAOYSA-N 0.000 claims 1
- BZLUACGIDLBVAR-UHFFFAOYSA-N N-(diaminomethylidene)-2-(3-oxo-2-propyl-1H-isoindol-1-yl)propanamide Chemical compound C1=CC=C2C(=O)N(CCC)C(C(C)C(=O)NC(N)=N)C2=C1 BZLUACGIDLBVAR-UHFFFAOYSA-N 0.000 claims 1
- UGVZLHOQNVDUCU-UHFFFAOYSA-N N-(diaminomethylidene)-2-(5,6-dichloro-2-cyclopropyl-3-oxo-1H-isoindol-1-yl)acetamide Chemical compound O=C1C2=CC(Cl)=C(Cl)C=C2C(CC(=O)NC(=N)N)N1C1CC1 UGVZLHOQNVDUCU-UHFFFAOYSA-N 0.000 claims 1
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- ZQMVRCIHVKTUGS-SECBINFHSA-N N-(diaminomethylidene)-2-[(1R)-3-oxo-2-(2,2,2-trifluoroethyl)-6-(trifluoromethyl)-1H-isoindol-1-yl]acetamide Chemical compound C1=C(C(F)(F)F)C=C2[C@@H](CC(=O)NC(=N)N)N(CC(F)(F)F)C(=O)C2=C1 ZQMVRCIHVKTUGS-SECBINFHSA-N 0.000 claims 1
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- 150000004791 alkyl magnesium halides Chemical class 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000005418 aryl aryl group Chemical group 0.000 claims 1
- 125000004429 atoms Chemical group 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 150000001718 carbodiimides Chemical class 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 230000000747 cardiac effect Effects 0.000 claims 1
- 231100000457 cardiotoxic Toxicity 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 230000001472 cytotoxic Effects 0.000 claims 1
- 239000002254 cytotoxic agent Substances 0.000 claims 1
- 239000000032 diagnostic agent Substances 0.000 claims 1
- 125000005842 heteroatoms Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- KLGZELKXQMTEMM-UHFFFAOYSA-N hydride Chemical compound [H-] KLGZELKXQMTEMM-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
- 150000007517 lewis acids Chemical class 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 239000002831 pharmacologic agent Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VKMGSWIFEHZQRS-NSHDSACASA-N (1R)-1-(3,4-dichlorophenyl)-2-(propan-2-ylamino)ethanol Chemical compound CC(C)NC[C@H](O)C1=CC=C(Cl)C(Cl)=C1 VKMGSWIFEHZQRS-NSHDSACASA-N 0.000 description 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- BBAJPPCDTUZGNX-UHFFFAOYSA-N 3-hydroxy-2-(2,2,2-trifluoroethyl)-5-(trifluoromethyl)-3H-isoindol-1-one Chemical compound C1=C(C(F)(F)F)C=C2C(O)N(CC(F)(F)F)C(=O)C2=C1 BBAJPPCDTUZGNX-UHFFFAOYSA-N 0.000 description 1
- VYEWZIGLODHOPI-UHFFFAOYSA-N 3-hydroxy-2-(2,2,2-trifluoroethyl)-6-(trifluoromethyl)-3H-isoindol-1-one Chemical compound FC(F)(F)C1=CC=C2C(O)N(CC(F)(F)F)C(=O)C2=C1 VYEWZIGLODHOPI-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 102100018344 PRPF3 Human genes 0.000 description 1
- 101700055558 PRPF3 Proteins 0.000 description 1
- 101710005260 RPL6A Proteins 0.000 description 1
- 101710005264 RPL6B Proteins 0.000 description 1
- GGUBFICZYGKNTD-UHFFFAOYSA-N Triethyl phosphonoacetate Chemical compound CCOC(=O)CP(=O)(OCC)OCC GGUBFICZYGKNTD-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- RPCNYKISXCFSJH-UHFFFAOYSA-N ethyl 2-[3-oxo-2-(2,2,2-trifluoroethyl)-5-(trifluoromethyl)-1H-isoindol-1-yl]acetate Chemical compound FC(F)(F)C1=CC=C2C(CC(=O)OCC)N(CC(F)(F)F)C(=O)C2=C1 RPCNYKISXCFSJH-UHFFFAOYSA-N 0.000 description 1
- CNNPUSRKNQQCNZ-UHFFFAOYSA-N ethyl 2-[3-oxo-2-(2,2,2-trifluoroethyl)-6-(trifluoromethyl)-1H-isoindol-1-yl]acetate Chemical compound C1=C(C(F)(F)F)C=C2C(CC(=O)OCC)N(CC(F)(F)F)C(=O)C2=C1 CNNPUSRKNQQCNZ-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- BZKBCQXYZZXSCO-UHFFFAOYSA-N sodium hydride Inorganic materials [H-].[Na+] BZKBCQXYZZXSCO-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0206783A FR2840302B1 (fr) | 2002-06-03 | 2002-06-03 | Derives d'isoindolones, procede de preparation et intermediaire de ce procede a titre de medicaments et compositions pharmaceutiques les renfermant |
| PCT/EP2003/005279 WO2003101450A1 (en) | 2002-06-03 | 2003-05-20 | N- ((3-oxo2, 3-dihydro-1h-isoindol-1-yl) acetyl) guanidine derivatives as nhe-1 inhibitors for the treatment of infarction and angina pectoris |
Publications (3)
| Publication Number | Publication Date |
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| JP2005533034A JP2005533034A (ja) | 2005-11-04 |
| JP2005533034A5 true JP2005533034A5 (de) | 2006-06-22 |
| JP4634793B2 JP4634793B2 (ja) | 2011-02-16 |
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| JP2004508808A Expired - Fee Related JP4634793B2 (ja) | 2002-06-03 | 2003-05-20 | 梗塞および狭心症の治療のためのｎｈｅ−１抑制剤としてのｎ−（（３−オキソ−２，３−ジヒドロ−１ｈ−イソインドール−１−イル）アセチル）グアニジン誘導体 |
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Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10356717A1 (de) * | 2003-12-02 | 2005-07-07 | Aventis Pharma Deutschland Gmbh | Verfahren zur Herstellung von (3-Oxo-2,3-dihydro-1H-isoindol-1-yl)-acetylguanidin-Derivaten |
| US7531569B2 (en) | 2003-12-02 | 2009-05-12 | Sanofi-Aventis Deutschland Gmbh | Process for preparing (3-oxo-2,3-dihydro-1H-isoindol-1-yl) acetylguanidine derivatives |
| KR100518184B1 (ko) * | 2003-12-27 | 2005-10-04 | 한국화학연구원 | 퓨란카보닐구아니딘 유도체, 그의 제조방법 및 그를포함하는 약학적 조성물 |
| TW200613272A (en) | 2004-08-13 | 2006-05-01 | Astrazeneca Ab | Isoindolone compounds and their use as metabotropic glutamate receptor potentiators |
| US7807706B2 (en) | 2005-08-12 | 2010-10-05 | Astrazeneca Ab | Metabotropic glutamate-receptor-potentiating isoindolones |
| US20070161648A1 (en) * | 2005-10-14 | 2007-07-12 | Hughes Terry V | Substituted dihydro-isoindolones useful in treating kinase disorders |
| TW200812962A (en) * | 2006-07-12 | 2008-03-16 | Astrazeneca Ab | New compounds I/418 |
| TWI417100B (zh) | 2007-06-07 | 2013-12-01 | Astrazeneca Ab | 二唑衍生物及其作為代謝型麩胺酸受體增效劑-８４２之用途 |
| US7790760B2 (en) | 2008-06-06 | 2010-09-07 | Astrazeneca Ab | Metabotropic glutamate receptor isoxazole ligands and their use as potentiators 286 |
| GB0811643D0 (en) | 2008-06-25 | 2008-07-30 | Cancer Rec Tech Ltd | New therapeutic agents |
| EP2588104B1 (de) | 2010-07-01 | 2014-12-10 | Merck Sharp & Dohme Corp. | Positive allosterische isoindolon-m1-rezeptormodulatoren |
| WO2013056015A1 (en) | 2011-10-14 | 2013-04-18 | Incyte Corporation | Isoindolinone and pyrrolopyridinone derivatives as akt inhibitors |
| CN103193794B (zh) * | 2013-04-12 | 2016-04-06 | 中国药科大学 | 一种异吲哚酮并异噁唑类稠环化合物及其合成方法 |
| GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
| GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
| CN106316922B (zh) * | 2016-08-17 | 2019-02-01 | 华东师范大学 | 一种含c-3全取代氧化吲哚衍生物及其合成方法和应用 |
| WO2018058109A1 (en) | 2016-09-26 | 2018-03-29 | Nusirt Sciences, Inc. | Compositions and methods for treating metabolic disorders |
| GB201704965D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| GB201704966D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| CN110664803B (zh) * | 2019-09-19 | 2023-08-29 | 中山大学 | 异吲哚酮类化合物在制备防治溶骨性疾病药物中的应用 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2107698T3 (es) * | 1993-02-20 | 1997-12-01 | Hoechst Ag | Benzoilguanidinas sustituidas, procedimiento para su preparacion, su utilizacion como medicamento, como inhibidores del intercambio celular de na+/h+ o como agente de diagnostico, asi como medicamento que las contiene. |
| FR2735166B1 (fr) * | 1995-06-08 | 1997-08-29 | Aerospatiale | Procede de fabrication d'un panneau ou analogue a proprietes structurale et acoustique et panneau ainsi obtenu |
| DE19737224A1 (de) * | 1997-08-27 | 1999-03-18 | Hoechst Marion Roussel De Gmbh | Pharmazeutisches Kombinationspräparat aus einem Inhibitor des Natrium-Wasserstoff-Austauschers und einem Arzneimittel zur Behandlung von Herz-Kreislauferkrankungen |
| DE19737463A1 (de) * | 1997-08-28 | 1999-03-04 | Hoechst Marion Roussel De Gmbh | Verwendung von Inhibitoren des Natrium-Wasserstoff-Austauschers zur Herstellung eines Arzneimittels zur Behandlung von Erkrankungen, die durch Protozoen verursacht werden |
| DE19738604A1 (de) * | 1997-09-04 | 1999-03-11 | Hoechst Marion Roussel De Gmbh | Die Verwendung von Hemmern des Natrium-Wasserstoff-Austauschers zur Herstellung eines Medikaments zur Verminderung der Giftigkeit cardiotoxischer Stoffe |
| ES2237080T3 (es) * | 1998-02-27 | 2005-07-16 | Pfizer Products Inc. | Derivados de n-((anillo di- o triaza dinsaturado de cinco miembros sustituido)carbonil)guanidina para el tratamiento de isquemia. |
| DE19859727A1 (de) * | 1998-12-23 | 2000-06-29 | Aventis Pharma Gmbh | Die Verwendung von Hemmern des Natrium-Wasserstoff-Austauschers zur Herstellung eines Medikaments zur Verhinderung von altersbedingten Organ-Dysfunktionen, altersbedingten Erkrankungen zur Lebensverlängerung |
| US6534651B2 (en) * | 2000-04-06 | 2003-03-18 | Inotek Pharmaceuticals Corp. | 7-Substituted isoindolinone inhibitors of inflammation and reperfusion injury and methods of use thereof |
| AP2002002651A0 (en) * | 2000-04-28 | 2002-12-31 | Pfizer Prod Inc | Sodium-hydrogen exchanger type 1 inhibitor (nhe-1) |
| DE10046993A1 (de) * | 2000-09-22 | 2002-04-11 | Aventis Pharma Gmbh | Substituierte Zimtsäureguanidide, Verfahren zur ihrer Herstellung, ihre Verwendung als Medikament sowie sie enthaltendes Medikament |
| ES2278016T3 (es) * | 2001-04-09 | 2007-08-01 | Novartis Vaccines And Diagnostics, Inc. | Compuestos guanidino como agonistas del receptor de melanocortina 4 (mc4-r). |
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